Aman Hospital and Research Center, Vadodara, India.
R&D Centre, Akay Natural Ingredients Pvt. Ltd., Cochin, India.
J Altern Complement Med. 2020 Oct;26(10):945-955. doi: 10.1089/acm.2020.0128. Epub 2020 Jul 14.
A combination of curcumagalactomannosides (CGM) (400 mg) with glucosamine hydrochloride (GLN) (500 mg) was evaluated against a standard dietary supplement combination chondroitin sulfate (CHN) (415 mg)/GLN (500 mg) for their effectiveness in alleviating the pain and symptoms among osteoarthritic subjects. Randomized, double-blinded and active-controlled study. The study was conducted in a hospital-based research center in Vadodara, Gujarat, India. Eighty subjects (38 males and 42 females), with confirmed osteoarthritis (OA) (Class I-III), were randomized into two parallel groups designated as Group I (CGM-GLN) and Group II (CHN-GLN). All the study subjects were supplemented with their corresponding intervention capsules (ether CGM along with GLN or CHN along with GLN), as a single oral dose twice a day, once in the morning 10-15 min before breakfast and again in the evening before dinner, for 84 days. A validated treadmill uphill walking protocol was used for the study, and the efficiency of supplementation was evaluated using visual analogue scale (VAS) score, Karnofsky Performance Scale (KPS) score, and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) questionnaire at the baseline, 28th, and 84th day following the treatment. Mechanism of action of CGM-GLN combination was analyzed by measuring the levels of serum inflammatory markers interleukin 1 beta (IL-1β), interleukin 6 (IL-6), and soluble vascular cell adhesion molecule-1 (sVCAM) at the baseline and 84th day. CGM-GLN was found to offer significant beneficial effects to pain, stiffness, and physical function of OA subjects compared with CHN-GLN, which was evident from the improvement in walking performance, VAS score, KPS score, and WOMAC score. The efficiency of CGM-GLN was almost double compared with the CHN-GLN by the end of the study (84th day). A significant reduction of inflammatory serum marker levels was observed among CGM-GLN subjects compared with CHN-GLN subjects. Compared with the baseline, CGM-GLN produced 54.52%, 59.08%, and 22.03% reduction in IL-1β, IL-6, and sVCAM levels, respectively. Whereas CHN-GLN group of subjects expressed only 23.17%, 21.38%, and 6.82% reduction in IL-1β, IL-6, and sVCAM levels, respectively. In conclusion, the present study demonstrated the potential benefits of CGM-GLN supplements in alleviating the symptoms and function of OA subjects compared with the standard CHN-GLN treatment. The augmented efficacy of CGM-GLN combination could be attributed to the enhanced anti-inflammatory effect of CGM.
姜黄素半乳甘露聚糖(CGM)(400mg)与盐酸氨基葡萄糖(GLN)(500mg)的联合用药与标准膳食补充剂硫酸软骨素(CHN)(415mg)/GLN(500mg)联合用药在缓解骨关节炎患者的疼痛和症状方面的有效性进行了评估。 这是一项随机、双盲和阳性对照研究。 该研究在印度古吉拉特邦巴罗达的一家医院研究中心进行。 80 名受试者(38 名男性和 42 名女性),确诊为骨关节炎(OA)(I-III 级),随机分为两组,分别指定为 I 组(CGM-GLN)和 II 组(CHN-GLN)。 所有研究对象均补充相应的干预胶囊(要么是 CGM 加 GLN,要么是 CHN 加 GLN),作为单次口服剂量,每天两次,一次在早上早餐前 10-15 分钟,另一次在晚上晚餐前,持续 84 天。 使用经过验证的跑步机上坡行走方案进行研究,并使用视觉模拟量表(VAS)评分、卡诺夫斯基表现量表(KPS)评分和西安大略和麦克马斯特大学骨关节炎指数(WOMAC)问卷评估补充剂的效率,基线时、第 28 天和第 84 天。在基线和第 84 天测量血清炎症标志物白细胞介素 1β(IL-1β)、白细胞介素 6(IL-6)和可溶性血管细胞黏附分子-1(sVCAM)的水平,分析 CGM-GLN 联合用药的作用机制。与 CHN-GLN 相比,CGM-GLN 为 OA 受试者的疼痛、僵硬和身体功能提供了显著的有益效果,这从行走表现、VAS 评分、KPS 评分和 WOMAC 评分的改善中可以看出。到研究结束(第 84 天)时,CGM-GLN 的效率几乎是 CHN-GLN 的两倍。与 CHN-GLN 组相比,CGM-GLN 组的血清炎症标志物水平显著降低。与基线相比,CGM-GLN 组的 IL-1β、IL-6 和 sVCAM 水平分别降低了 54.52%、59.08%和 22.03%。而 CHN-GLN 组的 IL-1β、IL-6 和 sVCAM 水平分别降低了 23.17%、21.38%和 6.82%。 总之,本研究表明,与标准 CHN-GLN 治疗相比,CGM-GLN 补充剂在缓解 OA 受试者的症状和功能方面具有潜在的益处。CGM-GLN 联合用药的增强疗效可能归因于 CGM 的增强抗炎作用。